Rapid Cognitive Deterioration in Progressive Supranuclear Palsy: A 1-Year Follow-Up Study
Xin-Yi Li1, Yu-Jie Yang2, Fang-Yang Jiao3
1Department of Neurology, National Clinical Research Center for Aging and Medicine, & National Center for Neurological Disorders, Huashan Hospital, Fudan University, Shanghai, China.
Movement Disorders Clinical Practice
|December 27, 2024
Summary
Progressive supranuclear palsy with Richardson syndrome (PSP-RS) shows faster cognitive decline than other PSP types. PSP-RS diagnosis is the main factor predicting mild cognitive impairment conversion to dementia within one year.
Area of Science:
- Neuroscience
- Neurology
- Clinical Research
Background:
- Cognitive impairment is a key symptom of progressive supranuclear palsy (PSP).
- Understanding cognitive decline in PSP subtypes is crucial for prognosis.
Purpose of the Study:
- To evaluate cognitive deterioration in different PSP subtypes over one year.
- To identify factors influencing disease prognosis in PSP patients.
Main Methods:
- Neuropsychological testing and 1-year follow-up of 117 PSP patients (PSPNI cohort).
- Classification into PSP-Richardson syndrome (PSP-RS) and PSP-non-RS.
- Categorization into normal cognition (PSP-NC), mild cognitive impairment (PSP-MCI), and PSP-dementia.
Main Results:
- At baseline, 30.8% had dementia, 53.0% MCI, and 16.2% NC.
- PSP-RS patients exhibited more severe motor and cognitive deficits, with faster progression in MMSE and visuospatial function.
- Twenty-seven of 62 PSP-MCI patients converted to dementia; PSP-RS diagnosis was the strongest predictor (HR=2.993).
Conclusions:
- PSP-RS patients experience more severe cognitive impairment and a faster longitudinal decline compared to PSP-non-RS.
- The PSP-RS subtype is the most significant factor contributing to the conversion of MCI to dementia within a 1-year period.
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